Contributions of humoral and cellular immunity to vaccine-induced protection in humans
Open accessAbstract
Vaccines play a vital role in protecting the host against infectious disease. The most effective licensed vaccines elicit long-term antigen-specific antibody responses by plasma cells in addition to the development of persisting T cell and B cell memory. The relative contributions of these different immune cell subsets are context-dependent and vary depending on the attributes of the vaccine (i.e., live/attenuated, inactivated, and subunit) as well as the biology of the pathogen in question. For relatively simple vaccines against bacterial antigens (e.g., tetanus toxin) or invariant viruses, the immunological correlates of protection are well-characterized. For more complex vaccines against viruses, especially those that mutate or cause latent infections, it is more difficult to define the specific correlates of immunity. This often requires observational/natural history studies, clinical trials, or experimental evaluation in relevant animal models in order for immunological correlates to be determined or extrapolated. In this review, we will discuss the relative contributions of virus-specific T cell and B cell responses to vaccine-mediated protection against disease.
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Protection afforded by currently licensed vaccines is primarily based on induction of a humoral immune response.
“Protection afforded by currently licensed vaccines is primarily based on induction of a humoral immune response (Amanna & Slifka, 2011).”
From mRNA mediates passive vaccination against infectious agents, toxins, and tumors (2017) · cites this paper as Amanna & Slifka, 2011
The section “Persisting antibody following vaccination; the first line of defense against infection” says antibody responses are the probable basis of efficacy for many of today’s most successful vaccines. But the Abstract and Conclusions say the relative contribution of humoral immunity depends on the vaccine and pathogen, and that protection often also involves cellular immunity. The claim extends the antibody-based account to currently licensed vaccines generally. (LLM, conf=0.85)
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Flagged first, then by citations
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- Gershon AA Takahashi M Seward JF Plotkin SA Orenstein WA Offit PA 2008 Varicella vaccine Vaccines 915 958 Saunders/Elsevier Philadelphia, PA
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Cited by
Sorted by citations
Tam, H. H., Melo, M. B., Kang, M., Pelet, J. M., Ruda, V. M., Foley, M. H., Hu, J. K., Kumari, S., Crampton, J., Baldeon, A. D., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1606050113 · Cited by 425 · see citing works
mRNA mediates passive vaccination against infectious agents, toxins, and tumors
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“Protection afforded by currently licensed vaccines is primarily based on induction of a humoral immune response (Amanna & Slifka, 2011).”
BackgroundEngineering humoral immunity as prophylaxis or therapy
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SARS-CoV-2 Transmission Risk to Household and Family Contacts by Vaccinated Healthcare Workers
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- Authors
- Amanna, I. J., & Slifka, M. K.
- Affiliations
- Najít Technologies (United States) (US)
- Oregon Health & Science University (US)
- Venue
- Virology
- Publisher
- Elsevier BV
- Published
- 2011-03
- Volume
- 411
- Issue
- 2
- Pages
- 206-215
- ISSN
- 0042-6822 (ISSN-L)
- PMC
- PMC3238379
- OpenAlex
- W2043944957
- Cited by
- 263
- References
- 169
- Citations by year
- 2026: 16 · 2025: 18 · 2024: 19 · 2023: 25 · 2022: 29 · 2021: 23 · 2020: 14 · 2019: 15 · 2018: 19 · 2017: 14 · 2016: 14 · 2015: 8 · 2014: 11 · 2013: 20 · 2012: 11
- FWCI
- 1.42
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Virology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Allergy and Infectious Diseases, National Institutes of Health (R43 AI079898, UO1 AI082196, U54 AI081680)
- ONPRC (RR00163)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune responses and vaccinations
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Keywords
- vaccine-induced immunity, humoral immunity, cell-mediated immunity, T cell response, B cell response, immunological correlates of protection, vaccine types, virus-specific immunity, memory B cells, plasma cells
- MeSH terms
- B-Lymphocytes, Humans, Immunity, Cellular, T-Lymphocytes, Viral Vaccines, Immunity, Humoral
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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